ENST00000461574.2:c.5360G>A
|
ENSP00000417241.2:p.Gly1787Asp
|
|
ENST00000470026.6:c.5363G>A
|
ENSP00000419274.2:p.Gly1788Asp
|
|
ENST00000473961.6:c.5237G>A
|
ENSP00000420201.2:p.Gly1746Asp
|
|
ENST00000476777.6:c.5357G>A
|
ENSP00000417554.2:p.Gly1786Asp
|
|
ENST00000477152.6:c.5285G>A
|
ENSP00000419988.2:p.Gly1762Asp
|
|
ENST00000478531.6:c.2051G>A
|
ENSP00000420412.2:p.Gly684Asp
|
|
ENST00000489037.2:c.5285G>A
|
ENSP00000420781.2:p.Gly1762Asp
|
|
ENST00000493919.6:c.1913G>A
|
ENSP00000418819.2:p.Gly638Asp
|
|
ENST00000494123.6:c.5363G>A
|
ENSP00000419103.2:p.Gly1788Asp
|
|
ENST00000497488.2:c.4475G>A
|
ENSP00000418986.2:p.Gly1492Asp
|
|
ENST00000618469.2:c.5363G>A
|
ENSP00000478114.2:p.Gly1788Asp
|
|
ENST00000634433.2:c.5240G>A
|
ENSP00000489431.2:p.Gly1747Asp
|
|
ENST00000644379.2:c.5429G>A
|
ENSP00000496570.2:p.Gly1810Asp
|
|
ENST00000644555.2:c.1913G>A
|
ENSP00000494614.2:p.Gly638Asp
|
|
ENST00000652672.2:c.5222G>A
|
ENSP00000498906.2:p.Gly1741Asp
|
|
ENST00000484087.6:c.1925G>A
|
ENSP00000419481.2:p.Gly642Asp
|
|
ENST00000700081.1:n.1246G>A
|
|
|
ENST00000357654.9:c.5363G>A
MANE Select
|
ENSP00000350283.3:p.Gly1788Asp
|
|
ENST00000471181.7:c.5426G>A
|
ENSP00000418960.2:p.Gly1809Asp
|
|
ENST00000644379.1:c.1750G>A
|
|
|
ENST00000352993.7:c.1937G>A
|
ENSP00000312236.5:p.Gly646Asp
|
|
ENST00000357654.7:c.5363G>A
|
ENSP00000350283.3:p.Gly1788Asp
|
|
ENST00000461221.5:c.*5146G>A
|
ENSP00000418548.1:n.*5146G>A
|
|
ENST00000468300.5:c.2021-1461G>A
|
ENSP00000417148.1:n.2021-1461G>A
|
|
ENST00000471181.6:c.5426G>A
|
ENSP00000418960.2:p.Gly1809Asp
|
|
ENST00000491747.6:c.2051G>A
|
ENSP00000420705.2:p.Gly684Asp
|
|
ENST00000493795.5:c.5222G>A
|
ENSP00000418775.1:p.Gly1741Asp
|
|
ENST00000586385.5:c.293G>A
|
ENSP00000465818.1:p.Gly98Asp
|
|
ENST00000591534.5:c.836G>A
|
ENSP00000467329.1:p.Gly279Asp
|
|
ENST00000591849.5:c.62G>A
|
ENSP00000465347.1:p.Gly21Asp
|
|
NM_007294.3:c.5363G>A , LRG_292t1:c.5363G>A
|
NP_009225.1:p.Gly1788Asp
|
|
NM_007297.3:c.5222G>A
|
NP_009228.2:p.Gly1741Asp
|
|
NM_007298.3:c.2051G>A
|
NP_009229.2:p.Gly684Asp
|
|
NM_007299.3:c.2021-1461G>A
|
NP_009230.2:n.2021-1461G>A
|
|
NM_007300.3:c.5426G>A
|
NP_009231.2:p.Gly1809Asp
|
|
NR_027676.1:n.5499G>A
|
|
|
NM_007294.4:c.5363G>A
MANE Select
|
NP_009225.1:p.Gly1788Asp
|
|
NM_007297.4:c.5222G>A
|
NP_009228.2:p.Gly1741Asp
|
|
NM_007299.4:c.2021-1461G>A
|
NP_009230.2:n.2021-1461G>A
|
|
NM_007300.4:c.5426G>A
|
NP_009231.2:p.Gly1809Asp
|
|
NR_027676.2:n.5540G>A
|
|
|